泛素化和降解过程涉及一系列蛋白和泛素。
Ubiquitylation and degradation involve a complex set of proteins in addition to ubiquitin.
泛素在目标蛋白上形成多分子长链是多聚泛素化的开始。
Ubiquitin can form chains consisting of several molecules attached to a target protein to form polyubiquitylation.
标记并欺骗诱导过分活化一个被称为泛素化的细胞程序。
Marked for Disposal The trick is played out in a cell process called ubiquitylation.
在一些植物病毒和动物病毒中发现了泛素相关蛋白或泛素化病毒蛋白。
Ubiquitin-related proteins and ubiquitined vims proteins have been found in some plant viruses and animal viruses.
此损害导致大量多泛素化蛋白的积聚和线粒体功能障碍（被公认的细胞死亡的媒介）。
This impairment resulted in massive accumulation of polyubiquitinated proteins and of dysfunctional mitochondria which are the putative mediators of cell death.
SUMO的生化反应途径与泛素化有类似之处，但不同的是会使蛋白质更加稳定。而不是降解蛋白质。
The biochemical effects of SUMO are somehow similar with those of ubiquitin, but SUMO stabilizes proteins, not degrades.
泛素对蛋白的修饰又叫泛素化，它能极大地影响很多细胞内调控过程，该发现获得了2004年诺贝尔奖。
Modification of proteins by ubiquitin -the so-called ubiquitylation - is of greatest importance in many regulatory processes in the cell and its discovery was awarded the Nobel Prize in 2004.
本研究确定了主要的组蛋白h 2 A去泛素和表明H2A去泛素化是至关重要参与细胞周期进程和基因表达。
This study identifies the major deubiquitinase for histone H2A and demonstrates that H2A deubiquitination is critically involved in cell cycle progression and gene expression.
泛素化在细胞生命活动的许多进程中发挥着至关重要的作用，其中包括激素信号和极端环境信号的感受和传导。
Ubiquitination plays important roles in regulating diverse cellular process in plants, including perception and signal transduction of various hormone and external environmental signals.
鼠单抗识别单泛素、多泛素和泛素化蛋白，这一抗体可能会与重组NEDD8发生交叉反应。种属特异性：所有种属。
Ubiquitin (P4D1) Mouse mAb detects ubiquitin, polyubiquitin and ubiquitinated proteins. This antibody may cross-react with recombinant NEDD8. Species Reactivity: All Species Expected.
IAA蛋白的泛素化降解在生长素反应中发挥关键性作用，ARF和AUX/IAA蛋白相互作用调节生长素响应基因的转录。
The degradation of AUX/IAA protein by ubiquitination plays essential role in auxin response, and the interaction between ARF and AUX/IAA protein regulates the transcription of auxin-response genes.
IRF7的活性可能受到乙酰化、泛素化和类泛素化修饰的调控，而这些修饰一般都发生在赖氨酸残基，我们猜测，赖氨酸残基在IRF7的修饰过程中可能具有重要的作用。
Since these modifications usually happen on lysine residues of target proteins, we assumed that the functions of IRF7 could be highly affected by the mutation of lysine residues.
IRF7的活性可能受到乙酰化、泛素化和类泛素化修饰的调控，而这些修饰一般都发生在赖氨酸残基，我们猜测，赖氨酸残基在IRF7的修饰过程中可能具有重要的作用。
Since these modifications usually happen on lysine residues of target proteins, we assumed that the functions of IRF7 could be highly affected by the mutation of lysine residues.
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